Canonical Allele Identifier: CA2770491066

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270181_31270182insCA , CM000668.2:g.31270181_31270182insCA	GRCh38
NC_000006.11:g.31237958_31237959insCA , CM000668.1:g.31237958_31237959insCA	GRCh37
NC_000006.10:g.31345937_31345938insCA	NCBI36
NG_029422.2:g.6950_6951insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.895+28_895+29insTG MANE Select	ENSP00000365402.5:n.895+28_895+29insTG
ENST00000376228.9:c.895+28_895+29insTG	ENSP00000365402.5:n.895+28_895+29insTG
ENST00000376237.8:c.*482+28_*482+29insTG	ENSP00000365412.4:n.*482+28_*482+29insTG
ENST00000383329.7:c.895+28_895+29insTG	ENSP00000372819.3:n.895+28_895+29insTG
ENST00000470363.5:n.213+28_213+29insTG
ENST00000487245.5:n.1254+28_1254+29insTG
NM_002117.5:c.895+28_895+29insTG	NP_002108.4:n.895+28_895+29insTG
NM_002117.6:c.895+28_895+29insTG MANE Select	NP_002108.4:n.895+28_895+29insTG